Nidhal K. Maraie
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Application of Nanoemulsion Technology for Preparation and Evaluation of Intranasal Mucoadhesive Nano- In-situ Gel for Ondansetron Hcl Nidhal K. Maraie
Journal of Global Pharma Technology .
Publisher : Journal of Global Pharma Technology

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Objective: Developing more effective and promising in situ gel nasal preparation for ondansetron HCl (OND-HCl) using nanoemulsion (NE) technology and study all the parameters that can optimize the final formula. Method: Screening of oils, surfactants and co-surfactants was performed on the basis of OND-HCl solubility and NE area of emulsifier ratio (Smix), respectively. Pseudo-ternary phase diagrams were constructed by aqueous titration method. Twelve NE formulas were prepared by ultrasonic emulsification and characterized for droplet size, zeta potential, polydispersity index, separation, conductivity, TEM, % transmittance, dilution and visual transparency. The best NE formulation was selected and applied to prepare nano-in situ gel (NIG) using poloxamer 407 as thermoreversible polymer, chitosan and HPMC E15 as mucoadhesive polymers.  The six NIG formulas were evaluated for pH, drug content, osmolarity, gelation temperature, mucoadhesive force, viscosity and in vitro drug release.  Results: The mean droplet size, polydispersity index, zeta potential, conductivity and % transmittance for the selected NE formula (F11) were found to be 64.87 nm, 0.544, - 0.146, 210 μS/cm, and 99.08% respectively. The gelation temperatures, pH, drug content, osmolarity and mucoadhesive force for the selected  NIG formula (NIG6) were 33 ºC, 5.8, 99.215%, 106.06 mOsmol/l (0.62%), 7372.21 dyne/cm² respectively. The in vitro drug release study of NIG6 showed 100% after 6h.  Conclusion: The results of this work indicated the possibility of application of NE technology in the formulation of NIG that has good mucoadhesive force to prolong the preparation residence time in the nose.Keywords: Chitosan, Nano-in situ gel, HPMCE15, Nanoemulsion, Ondansetron HCl.
Application of Proniosomal Powder Technology to Prepare Fast Water Dissolving Tablets for Dutasteride Nidhal K. Maraie
Journal of Global Pharma Technology .
Publisher : Journal of Global Pharma Technology

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Objective: The aim of the study is to prepare fast water dissolving dutasteride tablets containing a pronisomal powder that yield niosomal dispersion of dutasteride upon dissolving in hot water. The niosomes derived from dissolved tablets may improve the dissolution and permeability of dutasteride since it is loaded in the niosomal vesicles and avoid the high cost and other disadvantages of the soft gelatin capsules commercially available. Method: Ten formulas of dutasteride proniosomal gels were prepared by coaservation method and niosomes derived from them were evaluated for their loading capacity, particle size, particle size distribution , zeta-potential and in-vitro drug release in order to determine the optimum type and quantity of proniosomal contents that will be used to prepare maltodextrin based proniosmal powder formulas which were evaluated and the optimum proniosomal powder formula was used to prepare dutasteride tablet. Results: Thickness, , hardness, disintegration time and in-vitro drug release for the optimum dutasteride tablet T5 were 5.57±0.08 mm, 3.1±0.11 Kg/cm2, 2.9±0.03 and reaches 100% release after 30 min. Particle size, polydispersity index (PDI), and zeta potential of niosomes derived from dissolving dutasteride tablet (T5) were ~263±3.8 nm, 0.225, and -5.43±0.436 mV Conclusion: This results indicating the contribution niosomes derived from proniosomal powder in improving the dutasteride solubility and gave higher dissolution rate compared to the conventional soft gelatin capsule of the same drug . Therefore presenting an oral dosage form that is more convenient and having all the advantage of tablets. Keywords: Cholesterol, Dutasteride, Niosomes, Proniosomes, Span 60, and Tween 20.